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Alpha-synuclein haplotypes implicated in risk of Parkinson's disease.
Tan EK, Chai A, Teo YY, Zhao Y, Tan C, Shen H, Chandran VR, Teoh ML, Yih Y, Pavanni R, Wong MC, Puvan K, Lo YL, Yap E. Tan EK, et al. Among authors: shen h. Neurology. 2004 Jan 13;62(1):128-31. doi: 10.1212/01.wnl.0000101721.25345.dc. Neurology. 2004. PMID: 14718715
Analysis of LRRK2 functional domains in nondominant Parkinson disease.
Skipper L, Shen H, Chua E, Bonnard C, Kolatkar P, Tan LC, Jamora RD, Puvan K, Puong KY, Zhao Y, Pavanni R, Wong MC, Yuen Y, Farrer M, Liu JJ, Tan EK. Skipper L, et al. Among authors: shen h. Neurology. 2005 Oct 25;65(8):1319-21. doi: 10.1212/01.wnl.0000180517.70572.37. Neurology. 2005. PMID: 16247070
Genetic analysis of Nurr1 haplotypes in Parkinson's disease.
Tan EK, Chung H, Zhao Y, Shen H, Chandran VR, Tan C, Teoh ML, Yih Y, Pavanni R, Wong MC. Tan EK, et al. Among authors: shen h. Neurosci Lett. 2003 Aug 28;347(3):139-42. doi: 10.1016/s0304-3940(03)00539-1. Neurosci Lett. 2003. PMID: 12875905
Nurr1 mutational screen in Parkinson's disease.
Tan EK, Chung H, Chandran VR, Tan C, Shen H, Yew K, Pavanni R, Puvan KA, Wong MC, Teoh ML, Yih Y, Zhao Y. Tan EK, et al. Among authors: shen h. Mov Disord. 2004 Dec;19(12):1503-5. doi: 10.1002/mds.20246. Mov Disord. 2004. PMID: 15390059
Case-control study of UCHL1 S18Y variant in Parkinson's disease.
Tan EK, Puong KY, Fook-Chong S, Chua E, Shen H, Yuen Y, Pavanni R, Wong MC, Puvan K, Zhao Y. Tan EK, et al. Among authors: shen h. Mov Disord. 2006 Oct;21(10):1765-8. doi: 10.1002/mds.21064. Mov Disord. 2006. PMID: 16941465
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